Association between missense variants of uncertain significance in the CHEK2 gene and hereditary breast cancer: a cosegregation and bioinformatics analysis

Y aquí el de predisposición a cáncer: https://t.co/Rt9pIb1i7o

Inherited CHEK2 gene mutations elevate #BreastCancer risk. In a study of 396 patients, 0.75% had pathogenic variants, and 1.77% had uncertain significance. Family history was present in all cases. Daily biotech insights 👉🏼 @gathersight. https://t.co/uDVjhk

RT @FrontGenetics: New Research: Association between missense variants of uncertain significance in the CHEK2 gene and hereditary breast ca…

RT @elHectro2: Uy, que casi se me olvida contaros, que me han publicado un paper hoy!!!! Por si queréis echar un ojo: https://t.co/Rt9pIb0…